 Connexin 30
"Connexin 30" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A gap junction beta subunit that forms heteromeric hemichannels when paired with alpha subunits such as connexin-40 or CONNEXIN 43. Mutations in the connexin 30 gene (GJ6B) are associated with CLOUSTON'S SYNDROME and some hereditary forms of deafness.
| Descriptor ID |
D000075302
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| MeSH Number(s) |
D12.776.543.585.250.150
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| Concept/Terms |
Connexin 30- Connexin 30
- Gap Junction beta-6 Protein
- Gap Junction beta 6 Protein
- CX30 Channels
- Channels, CX30
- GJB6 Protein
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Below are MeSH descriptors whose meaning is more general than "Connexin 30".
Below are MeSH descriptors whose meaning is more specific than "Connexin 30".
This graph shows the total number of publications written about "Connexin 30" by people in this website by year, and whether "Connexin 30" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 0 | 1 | 1 |
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Below are the most recent publications written about "Connexin 30" by people in Profiles.
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Putcha GV, Bejjani BA, Bleoo S, Booker JK, Carey JC, Carson N, Das S, Dempsey MA, Gastier-Foster JM, Greinwald JH, Hoffmann ML, Jeng LJ, Kenna MA, Khababa I, Lilley M, Mao R, Muralidharan K, Otani IM, Rehm HL, Schaefer F, Seltzer WK, Spector EB, Springer MA, Weck KE, Wenstrup RJ, Withrow S, Wu BL, Zariwala MA, Schrijver I. A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort. Genet Med. 2007 Jul; 9(7):413-26.
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